Clinic Versus Home Spirometry

Last updated: January 20, 2022
Sponsor: University of Nottingham
Overall Status: Active - Recruiting

Phase

N/A

Condition

Asthma

Treatment

N/A

Clinical Study ID

NCT05219773
288594
  • Ages 18-80
  • All Genders

Study Summary

The study aims to assess the differences between spirometry performed with the NuvoAir Air Next spirometer in the clinic setting with both direct and virtual supervision via a video call, and in the home setting with virtual supervision. This is will be achieved by comparing lung function values, specifically the FEV1 and FVC measurements. We also wish to evaluate participant's perceptions of home spirometry, by using a survey.

This is a multi-centre, cross-over study. The study will enrol participants with a diagnosis of asthma and COPD, across participating study sites until 68 have completed the study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • An ability to provide fully informed consent.
  • A diagnosis of asthma or COPD.
  • Male or female aged ≥18 and ≤ 80 years of age.

Exclusion

Exclusion Criteria:

  • Symptoms suggestive of COVID-19.
  • An exacerbation of asthma or COPD or symptoms of a respiratory infection within the 30days prior to the first visit.
  • Any other clinically significant medical disease or uncontrolled concomitant disease,that is likely, in the opinion of the Investigator(s), to impact on the ability toparticipate in the study.
  • The presence of any contraindications to spirometry.

Study Design

Total Participants: 68
Study Start date:
December 14, 2021
Estimated Completion Date:
May 31, 2022

Connect with a study center

  • Respiratory Research Unit

    Nottingham, Nottinghamshire NG51PB
    United Kingdom

    Active - Recruiting

  • Bradford Teaching Hospitals NHS Foundation Trust

    Bradford, BD9 6RJ
    United Kingdom

    Site Not Available

  • The Rotherham NHS Foundation Trust

    Rotherham, S60 2UD
    United Kingdom

    Site Not Available

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